Variant #0000564851 (NC_000018.9:g.43531186C>T, NM_020964.2:c.1271G>A (EPG5))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43531186C>T |
DNA change (hg38) |
g.45951220C>T |
Published as |
EPG5(NM_020964.2):c.1271G>A (p.(Ser424Asn)), EPG5(NM_020964.3):c.1271G>A (p.S424N) |
ISCN |
- |
DB-ID |
EPG5_000100 See all 4 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.01102 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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